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CYCLON and NPM1 Cooperate within an Oncogenic Network Predictive of R-CHOP Response in DLBCL.
Bouroumeau A, Bussot L, Hamaidia S, Garcìa-Sandoval A, Bergan-Dahl A, Betton-Fraisse P, Duley S, Fournier C, Aucagne R, Adrait A, Couté Y, McLeer A, Col E, David-Boudet L, Raskovalova T, Jacob MC, Vettier C, Chevalier S, Carras S, Lefebvre C, Algrin C, Gressin R, Callanan MB, Sartelet H, Bonnefoix T, Emadali A. Bouroumeau A, et al. Among authors: sartelet h. Cancers (Basel). 2021 Nov 24;13(23):5900. doi: 10.3390/cancers13235900. Cancers (Basel). 2021. PMID: 34885010 Free PMC article.
c-MYC and p53 expression highlight starry-sky pattern as a favourable prognostic feature in R-CHOP-treated diffuse large B-cell lymphoma.
Bouroumeau A, Bussot L, Bonnefoix T, Fournier C, Chapusot C, Casasnovas O, Martin L, McLeer A, Col E, David-Boudet L, Lefebvre C, Algrin C, Raskovalova T, Jacob MC, Vettier C, Chevalier S, Callanan MB, Gressin R, Emadali A, Sartelet H. Bouroumeau A, et al. Among authors: sartelet h. J Pathol Clin Res. 2021 Nov;7(6):604-615. doi: 10.1002/cjp2.223. Epub 2021 Aug 9. J Pathol Clin Res. 2021. PMID: 34374220 Free PMC article.
Extranucleolar CYCLON Staining Pattern Is Strongly Associated to Relapse/Refractory Disease in R-CHOP-treated DLBCL.
Bouroumeau A, Bussot L, Sartelet H, Fournier C, Betton-Fraisse P, Col E, David-Boudet L, McLeer A, Lefebvre C, Raskovalova T, Jacob MC, Vettier C, Chevalier S, Algrin C, Carras S, Gressin R, Callanan MB, Bonnefoix T, Emadali A. Bouroumeau A, et al. Among authors: sartelet h. Hemasphere. 2021 Jun 12;5(7):e598. doi: 10.1097/HS9.0000000000000598. eCollection 2021 Jul. Hemasphere. 2021. PMID: 34131636 Free PMC article. No abstract available.
Transformation of a low-grade follicular lymphoma into a composite lymphoma combining a high-grade B-cell lymphoma and a lymphoblastic neoplasm expressing Terminal deoxynucleotidyl Transferase: a case report.
Bouroumeau A, Kaphan E, Legrand C, Raskovalova T, Szymanski G, Vettier C, Lefebvre C, Jacob MC, McLeer A, Peuchmaur M, Gressin R, Sartelet H. Bouroumeau A, et al. Among authors: sartelet h. J Med Case Rep. 2020 Jul 27;14(1):117. doi: 10.1186/s13256-020-02433-6. J Med Case Rep. 2020. PMID: 32713346 Free PMC article.
High Activation of the AKT Pathway in Human Multicystic Renal Dysplasia.
Apostolou A, Poreau B, Delrieu L, Thévenon J, Jouk PS, Lallemand G, Emadali A, Sartelet H. Apostolou A, et al. Among authors: sartelet h. Pathobiology. 2020;87(5):302-310. doi: 10.1159/000509152. Epub 2020 Sep 14. Pathobiology. 2020. PMID: 32927453 Free article.
PBX1 haploinsufficiency leads to syndromic congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
Le Tanno P, Breton J, Bidart M, Satre V, Harbuz R, Ray PF, Bosson C, Dieterich K, Jaillard S, Odent S, Poke G, Beddow R, Digilio MC, Novelli A, Bernardini L, Pisanti MA, Mackenroth L, Hackmann K, Vogel I, Christensen R, Fokstuen S, Béna F, Amblard F, Devillard F, Vieville G, Apostolou A, Jouk PS, Guebre-Egziabher F, Sartelet H, Coutton C. Le Tanno P, et al. Among authors: sartelet h. J Med Genet. 2017 Jul;54(7):502-510. doi: 10.1136/jmedgenet-2016-104435. Epub 2017 Mar 7. J Med Genet. 2017. PMID: 28270404
Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction.
Petre G, Lorès P, Sartelet H, Truffot A, Poreau B, Brandeis S, Martinez G, Satre V, Harbuz R, Ray PF, Amblard F, Devillard F, Vieville G, Berger F, Jouk PS, Vaiman D, Touré A, Coutton C, Bidart M. Petre G, et al. Among authors: sartelet h. Clin Genet. 2018 Dec;94(6):575-580. doi: 10.1111/cge.13449. Epub 2018 Oct 17. Clin Genet. 2018. PMID: 30221343
123 results